Primary Site >> Esophagus Cancer

Gene >> BRCA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357654
Start 43092494:43092494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3037G>C
AA Mutation p.Glu1013Gln(p.E1013Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000357654
Start 43095848:43095848(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.668A>C
AA Mutation p.Lys223Thr(p.K223T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000357654
Start 43090998:43090998(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs80356871
CDS Mutation c.4131C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000357654
Start 43051097:43051097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5298C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000357654
Start 43124034:43124034(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.63C>T
Mutation Classification Silent
Feature Type Transcript